(E)-tetradec-3-enol

  • Name: (E)-tetradec-3-enol
  • CAS: 68900-86-7
  • Purity: 99%
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  • Molecular Formula: C14H28 O
  • Molecular Weight: 212.376
  • Vapor Pressure: 8.95E-05mmHg at 25°C 
  • Boiling Point: 303.4°C at 760 mmHg 
  • Flash Point: 106.4°C 
  • PSA： 20.23000 
  • Density: 0.846g/cm3 
  • LogP: 4.45580 

(E)-tetradec-3-enol(Cas 68900-86-7) Usage

General Description

(E)-tetradec-3-enol, also known as (E)-3-tetradecen-1-ol, is a chemical compound with the molecular formula C14H28O. It is a colorless to pale yellow liquid with a floral, waxy, and green odor. (E)-tetradec-3-enol is commonly found in natural products such as flowers, fruits, and vegetables, and is often used as a flavor and fragrance ingredient in the food and cosmetic industries. It is also known to have potential insecticidal and antimicrobial properties, making it a useful compound for pest control and preservation applications. (E)-tetradec-3-enol is a versatile compound with various industrial and agricultural uses, making it a valuable asset in the chemical and scientific communities.

InChI:InChI=1/C14H28O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h11-12,15H,2-10,13-14H2,1H3/b12-11+

68900-86-7 Relevant articles

Method for synthesizing cis-3-tetradecanoacetate and trans-3-tetradecanoacetate

-

Paragraph 0033; 0039; 0040; 0045; 0050; 0051, (2019/08/01)

The invention discloses a method for syn...

Tandem IBX-Promoted Primary Alcohol Oxidation/Opening of Intermediate β,γ-Diolcarbonate Aldehydes to (E)-γ-Hydroxy-α,β-enals

Kumari, Anupama,Gholap, Sachin P.,Fernandes, Rodney A.

, p. 2278 - 2290 (2019/06/17)

A tandem IBX-promoted oxidation of prima...

Short and stereoselective synthesis of (E)-3-alkenyl acetates, insect sex pheromone constituents of Lepidoptera; Gelechidae

Ragoussis, Valentine,Vamvaka, Ekaterini,Kolymbadi, Maria

, p. 398 - 399 (2007/10/03)

(E)-3-alkenyl acetates, which are insect...

Metal/Ammonia Reduction of Ethers of 3-Decyn-1-ol: Effects of Structure and Conditions on Cleavage and Rearrangement

Doolittle, Robert E.,Patrick, Delrea G.,Heath, Robert H.

, p. 5063 - 5066 (2007/10/02)

Reduction of the THP, ethyl, tert-butyl ...

68900-86-7 Process route

1-hydroxy-tetradec-3-yne
55182-74-6

1-hydroxy-tetradec-3-yne

trans-3-tetradecen-1-ol
68900-86-7

trans-3-tetradecen-1-ol

Conditions
Conditions Yield
With lithium aluminium tetrahydride; In diethylene glycol dimethyl ether; at 145 ℃; for 14h;
99.7%
With lithium aluminium tetrahydride; In diethylene glycol dimethyl ether; at 100 ℃; for 8h;
95.5%
With lithium aluminium tetrahydride; In diethylene glycol dimethyl ether; at 100 ℃; for 12h;
94%
trans-3-tetradecenoic acid
75730-21-1,6269-40-5

trans-3-tetradecenoic acid

trans-3-tetradecen-1-ol
68900-86-7

trans-3-tetradecen-1-ol

Conditions
Conditions Yield
With sodium bis(2-methoxyethoxy)aluminium dihydride; In diethyl ether; at 5 - 20 ℃;
76%

68900-86-7 Upstream products

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    1-hydroxy-tetradec-3-yne

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    trans-3-tetradecen-1-ol acetate

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